We will soon be closing our office again to carry out much needed improvements. These improvements will make our office a better work space, which is more accessible and will have more welcoming spaces for service users.
The office will be closed from Monday 17th May to Monday 26th July 2021.
Even though our office is closed, business will continue as usual – Click here to find out more
As you have probably seen on the news, COVID-19 is a new illness that can affect your lungs and airways. It’s caused by a virus called coronavirus.
For guidance and advice about coronavirus and sickle cell view our guidance page: www.sicklecellsociety.org/coronavirus-and-scd/
Reverse Psychology London is partnering with the Sickle Cell Society to host ‘Rise Up For Sickle Cell’ a glamorous evening of celebration and fundraising on Wednesday 14th July 2021.
Join us for an evening of music, art, fashion, food and more at the exclusive Home House private members club. Find out more here: www.sicklecellsociety.org/riseup/
South London Gives & Give Blood, Spread Love is the Sickle Cell Society’s blood donation awareness project. The project’s goals are to engage individuals and communities from African and Caribbean backgrounds to become aware of the need for ethnically matched blood to treat people with sickle cell disorder.
For many people, fundraising online is the easiest way to support the causes you love. We’ve created a range of great options which you can use to support our work. We have broken it down into three categories to help you make the best out of your fundraising.
New Updated Edition of ‘Sickle Cell Disease in Childhood: Standards and Recommendations for Clinical Care’
The 3rd edition of the paediatric standards has just been published to support paediatricians, haematologists, specialist nurses and psychologists, and those responsible for monitoring outcomes i.e. hospital trusts, commissioning authorities and peer-review services.
Download here: www.sicklecellsociety.org/paediatricstandards/
This can only be achieved if funding is made available to educate health carers and other professionals about the condition. The Society aims to provide this. The Society does not discriminate between the types of sickle cell disorders or the ethnic groups concerned…